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Metal complexes of uracil derivatives with cytotoxicity and superoxide scavenging activity

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dc.contributor.author Prachayasittikul S.
dc.contributor.author Worachartcheewan A.
dc.contributor.author Pingaew R.
dc.contributor.author Suksrichavalit T.
dc.contributor.author Isarankura-Na-Ayudhya C.
dc.contributor.author Ruchirawat S.
dc.contributor.author Prachayasittikul V.
dc.date.accessioned 2021-04-05T03:34:25Z
dc.date.available 2021-04-05T03:34:25Z
dc.date.issued 2012
dc.identifier.issn 15701808
dc.identifier.other 2-s2.0-84858217824
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/14368
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84858217824&doi=10.2174%2f157018012799129918&partnerID=40&md5=ec25daa363a28ab424400767a86ceb54
dc.description.abstract 5-Substituted uracils were reported to be important core structure of diverse therapeutics. Herein, novel mixed ligand transition metal (Mn, Cu, Ni) complexes of 5-iodouracil (5Iu) with 8-hydroxyquinoline or 8HQ (1-3) and 5-nitrouracil (5Nu) with 8HQ (4-6) have been synthesized. The metal complexes 1-6 exert significant cytotoxicity against HepG2, A-549, HuCCA-1 and MOLT-3 cell lines. Particularly, the cytotoxicities of tested complexes against HepG2 cells show their IC 50 values lower than the reference drug. Cu complex of 5Nu (5Nu-Cu-8HQ, 5) is the most potent and promising cytotoxic compound. Mn complex of 5Iu (5Iu-Mn-8HQ, 1) is shown to be the most potent antioxidant. This finding reveals the application of using simple and commercially available bioactive ligands like 5Iu, 5Nu and 8HQ for the design and construction of new lead compounds with significant and promising bioactivities. © 2012 Bentham Science Publishers.
dc.subject 5 iodouracil 8 hydroxyquinoline copper complex
dc.subject 5 iodouracil 8 hydroxyquinoline manganese complex
dc.subject 5 iodouracil 8 hydroxyquinoline nickel complex
dc.subject 5 nitrouracil 8 hydroxyquinoline copper complex
dc.subject 5 nitrouracil 8 hydroxyquinoline manganese complex
dc.subject 5 nitrouracil 8 hydroxyquinoline nickel complex
dc.subject 8 quinolinol derivative
dc.subject copper complex
dc.subject doxorubicin
dc.subject etoposide
dc.subject fialuridine
dc.subject manganese derivative
dc.subject metal complex
dc.subject nickel complex
dc.subject scavenger
dc.subject superoxide
dc.subject superoxide dismutase
dc.subject unclassified drug
dc.subject uracil derivative
dc.subject acute lymphoblastic leukemia
dc.subject antioxidant activity
dc.subject article
dc.subject bile duct carcinoma
dc.subject cancer cell culture
dc.subject cell strain HepG2
dc.subject controlled study
dc.subject cytotoxicity
dc.subject drug potency
dc.subject drug structure
dc.subject drug synthesis
dc.subject human
dc.subject human tissue
dc.subject lung carcinoma
dc.subject priority journal
dc.title Metal complexes of uracil derivatives with cytotoxicity and superoxide scavenging activity
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Letters in Drug Design and Discovery. Vol 9, No.3 (2012), p.282-287
dc.identifier.doi 10.2174/157018012799129918


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